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Effect of Maternal Position Interventions on Vaginal Delivery Outcomes in Women with Fetal Occiput Posterior Position: A Randomized Controlled Trial

Effect of Cyclical Maternal Positioning on Spontaneous Vaginal Delivery Rate in Women with Fetal Occiput Posterior Position: A Prospective, Multicenter, Open-Label, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120729
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-03-31
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Occiput Posterior Position during Labor

Interventions

Intervention group:Participants in the intervention group were positioned in lateral recumbency with the maternal abdomen facing the opposite side of the fetal occiput. This position was maintained fo
Control group:The control group received routine care and were allowed to adopt any comfortable position, except for the specific positioning protocol used in the intervention group.

Sponsors

Xiamen Maternity and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Singleton, cephalic presentation, term pregnancy (37 to 41+6 weeks of gestation); 2. Nulliparous; 3. Active labor with cervical dilation of 3–5 cm, and diagnosis of occiput posterior position confirmed by both vaginal examination and ultrasound; 4. Category I fetal heart rate tracing; 5. Written informed consent obtained.

Exclusion criteria

Exclusion criteria: 1. Multiple pregnancy; 2. Estimated fetal weight >= 4000 g by prenatal ultrasound; 3. Abnormalities of the bony pelvis; 4. Prenatal diagnosis of polyhydramnios; 5. Prenatal diagnosis of oligohydramnios; 6. Severe maternal complications (e.g., chronic hypertension, heart disease, thrombocytopenia); 7. Inability to perform maternal positioning (e.g., lower limb musculoskeletal disorders); 8. Pregnancy complicated by psychiatric or psychological disorders; 9. Refusal to participate in the clinical study.

Design outcomes

Primary

MeasureTime frame
Vaginal delivery rate;

Secondary

MeasureTime frame
Instrumental vaginal delivery rate;Cesarean section rate;24-hour postpartum blood loss;Perineal laceration degree;Neonatal Apgar score;NICU admission rate;Neonatal birth injury rate;Duration of the first stage of labor;Duration of the second stage of labor;Rotation rate from OP to OA;Rate of oxytocin augmentation during active labor;

Countries

China

Contacts

Public ContactYang Meilin

Xiamen Maternity and Child Health Care Hospital

melin126@126.com+86 592 566 8203

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026